Canonical Allele Identifier: CA357984162

Gene: PITX2

Linked Data

• MyVariant Identifiers: chr4:g.111539706T>G (hg19) ; chr4:g.110618550T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.110618550T>G , CM000666.2:g.110618550T>G	GRCh38
NC_000004.11:g.111539706T>G , CM000666.1:g.111539706T>G	GRCh37
NC_000004.10:g.111759155T>G	NCBI36
NG_007120.1:g.23803A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000613094.5:c.323A>C	ENSP00000484763.2:p.Gln108Pro
ENST00000614423.5:c.448A>C	ENSP00000481951.2:p.Asn150His
ENST00000616641.5:n.516A>C
ENST00000644488.2:n.520A>C
ENST00000394595.8:c.529A>C	ENSP00000378095.4:p.Asn177His
ENST00000644488.1:n.592A>C
ENST00000644743.1:c.550A>C MANE Select	ENSP00000495061.1:p.Asn184His
ENST00000645131.1:n.481A>C
ENST00000306732.7:c.550A>C	ENSP00000304169.3:p.Asn184His
ENST00000354925.6:c.529A>C	ENSP00000347004.2:p.Asn177His
ENST00000355080.9:c.391A>C	ENSP00000347192.5:p.Asn131His
ENST00000394595.7:c.323A>C	ENSP00000378095.3:p.Gln108Pro
ENST00000394598.6:c.529A>C	ENSP00000378097.2:p.Asn177His
ENST00000511837.5:c.529A>C	ENSP00000421454.1:p.Asn177His
ENST00000556049.1:n.856A>C
ENST00000607868.1:n.277A>C
ENST00000613094.4:c.529A>C	ENSP00000484763.1:p.Asn177His
ENST00000614423.4:c.529A>C	ENSP00000481951.1:p.Asn177His
ENST00000616641.4:c.391A>C	ENSP00000484909.1:p.Asn131His
NM_000325.5:c.550A>C	NP_000316.2:p.Asn184His
NM_001204397.1:c.529A>C	NP_001191326.1:p.Asn177His
NM_001204398.1:c.529A>C	NP_001191327.1:p.Asn177His
NM_001204399.1:c.391A>C	NP_001191328.1:p.Asn131His
NM_153426.2:c.529A>C	NP_700475.1:p.Asn177His
NM_153427.2:c.391A>C	NP_700476.1:p.Asn131His
XM_006714235.2:c.529A>C	XP_006714298.1:p.Asn177His
XM_011532027.1:c.391A>C	XP_011530329.1:p.Asn131His
XM_024454090.1:c.196A>C	XP_024309858.1:p.Asn66His
NM_000325.6:c.550A>C MANE Select	NP_000316.2:p.Asn184His
NM_001204397.2:c.529A>C	NP_001191326.1:p.Asn177His
NM_153426.3:c.529A>C	NP_700475.1:p.Asn177His
NM_153427.3:c.391A>C	NP_700476.1:p.Asn131His